The reaction $$\mathrm{CO}(g)+\mathrm{H}_{2} \mathrm{O}(g) \rightleftharpoons \mathrm{H}_{2}(g)+\mathrm{CO}_{2}(g)$$ has an equilibrium constant of \(1.30\) at \(650^{\circ} \mathrm{C}\). Carbon monoxide and steam both have initial partial pressures of \(0.485 \mathrm{~atm}\), while hydrogen and carbon dioxide start with partial pressures of \(0.159\) atm. (a) Calculate the partial pressure of each gas at equilibrium. (b) Compare the total pressure initially with the total pressure at equilibrium. Would that relation be true of all gaseous systems?

Short Answer

Expert verified
Answer: No, it is not true for all gaseous systems. The initial and final total pressures are equal only when the total number of moles of gas remains constant, as in a reaction with equal stoichiometric coefficients on both sides of the equilibrium equation.

Step by step solution

01

(1. Write the equilibrium expression)

(First, we need to write the equilibrium expression for the given reaction. Based on the stoichiometry, the equilibrium constant (K) expression will be: $$K = \frac{P_{\mathrm{H_{2}}} P_{\mathrm{CO_{2}}}}{P_{\mathrm{CO}} P_{\mathrm{H_{2}O}}}$$)
02

(2. Define the change in partial pressures)

(To find the partial pressures at equilibrium, we should define the change in partial pressures for each species during the reaction. Let's denote the change in partial pressure as "x". We can represent the changes as follows: $$P_{\mathrm{CO}} = 0.485 - x$$ $$P_{\mathrm{H_{2}O}} = 0.485 - x$$ $$P_{\mathrm{H_{2}}} = 0.159 + x$$ $$P_{\mathrm{CO_{2}}} = 0.159 + x$$)
03

(3. Substitute the expressions into the equilibrium constant expression)

(Now, we can substitute the expressions for each partial pressure into the equilibrium constant expression: $$1.30 = \frac{(0.159 + x)(0.159 + x)}{(0.485 - x)(0.485 - x)}$$)
04

(4. Solve for x)

(Now, we should solve the equation for "x". This quadratic equation can be simplified as: $$1.30 (0.485 - x)^{2} = (0.159 + x)^{2}$$ Solve for x to find the either of the possible equilibrium values: $$x = 0.258$$ or $$x = -0.602$$ Since negative partial pressures are not possible, we should take the positive value for "x" as: $$x = 0.258$$)
05

(5. Calculate the partial pressures at equilibrium)

(With the value of "x" determined, we can now calculate the partial pressure of each species at equilibrium: $$P_{\mathrm{CO}} = 0.485 - 0.258 = 0.227 ~\mathrm{atm}$$ $$P_{\mathrm{H_{2}O}} = 0.485 - 0.258 = 0.227 ~\mathrm{atm}$$ $$P_{\mathrm{H_{2}}} = 0.159 + 0.258 = 0.417 ~\mathrm{atm}$$ $$P_{\mathrm{CO_{2}}} = 0.159 + 0.258 = 0.417 ~\mathrm{atm}$$)
06

(6. Compare the initial and final total pressures)

(Now, let's compare the total pressure initially and at equilibrium: Initial total pressure: $$P_{\mathrm{total}}^{initial} = P_{\mathrm{CO}}^{initial} + P_{\mathrm{H_{2}O}}^{initial} + P_{\mathrm{H_{2}}}^{initial} + P_{\mathrm{CO_{2}}}^{initial} = 0.485 + 0.485 + 0.159 + 0.159 = 1.288~\mathrm{atm}$$ Final total pressure: $$P_{\mathrm{total}}^{final} = P_{\mathrm{CO}}^{final} + P_{\mathrm{H_{2}O}}^{final} + P_{\mathrm{H_{2}}}^{final} + P_{\mathrm{CO_{2}}}^{final} = 0.227 + 0.227 + 0.417 + 0.417 = 1.288~\mathrm{atm}$$ The initial and equilibrium total pressures are equal, but this is not true for all gaseous systems. It is only the case when the total number of moles of gas remains constant, as in this particular reaction where the stoichiometric coefficients are equal on both sides of the equilibrium equation.)

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Most popular questions from this chapter

For the system $$\mathrm{PCl}_{5}(\mathrm{~g}) \rightleftharpoons \mathrm{PCl}_{3}(g)+\mathrm{Cl}_{2}(g)$$ \(K\) is 26 at \(300^{\circ} \mathrm{C}\). In a 5.0-L flask, a gaseous mixture consists of all three gases with partial pressures as follows: \(P_{\mathrm{PCl}_{5}}=0.012 \mathrm{~atm}, P_{\mathrm{Cl}_{2}}=0.45 \mathrm{~atm}\), \(P_{\mathrm{PCl}_{3}}=0.90 \mathrm{~atm} .\) (a) Is the mixture at equilibrium? Explain. (b) If it is not at equilibrium, which way will the system shift to establish equilibrium?

Benzaldehyde, a flavoring agent, is obtained by the dehydrogenation of benzyl alcohol. $$\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{OH}(g) \rightleftharpoons \mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CHO}(g)+\mathrm{H}_{2}(g)$$ \(K\) for the reaction at \(250^{\circ} \mathrm{C}\) is \(0.56\). If \(1.50 \mathrm{~g}\) of benzyl alcohol is placed in a 2.0-L flask and heated to \(250^{\circ} \mathrm{C}\), (a) what is the partial pressure of the benzaldehyde when equilibrium is established? (b) how many grams of benzyl alcohol remain at equilibrium?

At a certain temperature, \(K\) is \(1.3 \times 10^{5}\) for the reaction $$2 \mathrm{H}_{2}(g)+\mathrm{S}_{2}(g) \rightleftharpoons 2 \mathrm{H}_{2} \mathrm{~S}(g)$$ What is the equilibrium pressure of hydrogen sulfide if those of hydrogen and sulfur gases are \(0.103\) atm and \(0.417\) atm, respectively?

A sealed flask has \(0.541\) atm of \(\mathrm{SO}_{3}\) at \(1000 \mathrm{~K}\). The following equilibrium is established. $$2 \mathrm{SO}_{3}(g) \rightleftharpoons 2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g)$$ At equilibrium, the partial pressure of oxygen is measured to be \(0.216\) atm. Calculate \(K\) for the decomposition of \(\mathrm{SO}_{3}\) at \(1000 \mathrm{~K}\).

. Consider the equilibrium $$\mathrm{N}_{2}(g)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{NO}(g)$$ At a certain temperature, the equilibrium constant for the reaction is \(0.0255\). What are the partial pressures of all gases at equilibrium if the initial partial pressure of the gases (both reactants and products) is \(0.300 \mathrm{~atm} ?\)

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